Localized direct CP violation in B±→ρ0(ω)π±→π+π−π±B^\pm\rightarrow \rho^0 (\omega)\pi^\pm\rightarrow \pi^+ \pi^-\pi^\pm

We study the localized direct CP violation in the hadronic decays $B^\pm\rightarrow \rho^0 (\omega)\pi^\pm\rightarrow\pi^+ \pi^-\pi^\pm$, including the effect caused by an interesting mechanism involving the charge symmetry violating mixing between $\rho^0$ and $\omega$. We calculate the localized integrated direct CP violation when the low invariant mass of $\pi^+\pi^-$ [$m(\pi^+\pi^-)_{low}$] is near $\rho^0(770)$. For five models of form factors investigated, we find that the localized integrated direct CP violation varies from -0.0170 to -0.0860 in the ranges of parameters in our model when $0.750<m(\pi^+\pi^-)_{low}<0.800$\,GeV. This result, especially the sign, agrees with the experimental data and is independent of form factor models. The new experimental data shows that the signs of the localized integrated CP asymmetries in the regions $0.470<m(\pi^+\pi^-)_{low}<0.770$\,GeV and $0.770<m(\pi^+\pi^-)_{low}<0.920$\,GeV are positive and negative, respectively. We find that $\rho$-$\omega$ mixing makes the localized integrated CP asymmetry move towards the negative direction, and therefore contributes to the sign change in those two regions. This behavior is also model independent. We also calculate the localized integrated direct CP violating asymmetries in the regions $0.470<m(\pi^+\pi^-)_{low}<0.770$\,GeV and $0.770<m(\pi^+\pi^-)_{low}<0.920$\,GeV and find that they agree with the experimental data in some models of form factors.Comment: 22 pages, 2 figures. arXiv admin note: text overlap with arXiv:hep-ph/0602043, arXiv:hep-ph/0302156 by other author

Nucleation in binary polymer blends: Effects of foreign mesoscopic spherical particles

We study nucleation in binary polymer blends in the presence of mesoscopic spherical particles using self-consistent field theory, considering both heterogeneous and homogeneous nucleation mechanisms. Heterogeneous nucleation is found to be highly sensitive to surface selectivity and particle size, with rather subtle dependence on the particle size. Particles that preferentially adsorb the nucleating species generally favor heterogeneous nucleation. For sufficiently strong adsorption, barrierless nucleation is possible. By comparing the free energy barrier for homogeneous and heterogeneous nucleation, we construct a kinetic phase diagram